Clinical Affairs Manager

Support clinical evaluations for hearing instruments throughout the product lifecycle—from early product development through market launch and post-market activities—in accordance with Sonova procedures and applicable global regulations. Plan and scope clinical evaluations; identify, critically appraise and analyze relevant clinical and scientific data. Assess device safety, clinical performance and benefit–risk profile against the current state of the art. Create and maintain clinical evaluation documentation in collaboration with cross-functional project teams, including Clinical Evaluation Plans and Reports, Clinical Development Plans, scientific literature search plans and reports, and Post-Market Clinical Follow-up Plan and Reports. Support with regulatory guidance for product claims. Collaborate closely with Clinical Affairs, Clinical Operations, Audiology Research Centers, R&D, Regulatory Affairs, Quality and Marketing to ensure regulatory compliance, knowledge sharing and continuous process improvement.

At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear implants. We're dedicated to providing outstanding customer experiences through our global audiological care services, ensuring that everyone has the opportunity to engage fully with the world around them. Guided by a culture of continuous improvement that fosters resilience and self-motivation, our team is united by a shared commitment to excellence and a deep sense of pride in our work, each of us playing a vital role in creating meaningful change. Here you’ll find a diverse range of opportunities that span both consumer and medical solutions and the freedom to shape your career while making an impact on the lives of others. Join us in our mission to create a more connected world, where every voice is heard and every story matters.

• A master’s degree or PhD in health sciences, audiology, medicine, biomedical engineering, psychology, life sciences or a related field.

• Experience working with clinical studies or investigations, for example conducting, coordinating or monitoring clinical studies.

• Experience working with clinical data and the ability to critically interpret clinical study results, scientific publications and relevant statistical analyses.

• Experience conducting scientific literature searches using databases such as PubMed, Cochrane or Embase, as well as critically appraising and summarizing the identified evidence.

• Knowledge of relevant clinical and medical-device regulations and standards, such as EU MDR, FDA requirements, GCP or ISO 14155.

• Strong analytical skills and attention to detail.

• Ability to work independently, take ownership and manage responsibilities and deadlines effectively.

• A collaborative, self-motivated approach and the ability to communicate openly and effectively across interdisciplinary teams.

• Fluency in English is required; knowledge of German would be an advantage.